Cyclopropanemethanamine → HCID 68557991, compound
Reaction equation
[O:1]1[C:3]2([CH2:8][CH2:7][N:6]([C:9]([O:11][CH2:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[O:10])[CH2:5][CH2:4]2)[CH2:2]1.[CH:19]1([CH2:22][NH2:23])[CH2:21][CH2:20]1.Cl([O-])(=O)(=O)=O.[Li+]>>[CH:19]1([CH2:22][NH:23][CH2:2][C:3]2([OH:1])[CH2:8][CH2:7][N:6]([C:9]([O:11][CH2:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[O:10])[CH2:5][CH2:4]2)[CH2:21][CH2:20]1Participants
4
Procedure
The object product (2.53 g, 99%) was obtained in the same manner as in Example 24(1) and using benzyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate (1.98 g), 1-cyclopropylmethanamine (570 mg) and lithium perchlorate (960 mg).
Sources & evidence
- ORD record
- ord-86f0d69ce3094d098ece31f3c333a679
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08575167B2
Reaction notes
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